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. 2021 Oct;9(20):1524. doi: 10.21037/atm-21-4462

Table 3. Compounds detected and identified in negative ionization mode.

No. Retention time (min) Precursor m/z Identification Formula
1 2.0747 133.0178 D-(+)-Malic acid C4H6O5
2 5.384533 153.0214 Protocatechuic acid C7H6O4
3 6.345 787.2714 Eleutheroside E C34H46O18
4 6.714317 447.0975 Luteolin-7-O-glucoside C21H20O11
5 6.8433 431.1001 Vitexin C21H20O10
6 7.0098 121.0319 Benzoic acid C7H6O2
7 7.109283 189.0551 6,8-Dimethyl-4-hydroxycoumarin C11H10O3
8 7.197783 163.0432 P-Coumaric acid C9H8O3
9 8.282733 431.1031 5-Hydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one C21H20O10
10 8.501734 187.1008 Azelaic acid C9H16O4
11 8.584217 361.1675 Secoisolariciresinol C20H26O6
12 10.69313 593.153 Apigenin-6-C-glucoside-7-O-glucoside C27H30O15
13 11.4576 863.2072 Cosmosiin C21H20O10
14 16.85367 269.0463 Genistein C15H10O5
15 17.6438 269.0485 Emodin C15H10O5
16 19.35173 471.3476 Maslinic acid C30H48O4
17 22.29808 227.2043 Myristic acid C14H28O2
18 22.49942 253.22 9-Trans-palmitelaidic acid C16H30O2
19 22.8264 279.2355 Linoleic acid C18H32O2
20 24.01052 255.2355 Palmitic acid C16H32O2
21 24.1085 281.2527 Oleic acid C18H34O2